Results 1 to 10 of about 12,478 (189)
Glycoprotein Ib activation by thrombin stimulates the energy metabolism in human platelets. [PDF]
Thrombin-induced platelet activation requires substantial amounts of ATP. However, the specific contribution of each ATP-generating pathway i.e., oxidative phosphorylation (OxPhos) versus glycolysis and the biochemical mechanisms involved in the thrombin-
Norma Corona de la Peña +4 more
doaj +5 more sources
Antibiotic resistance mechanisms inform discovery: identification and characterization of a novel amycolatopsis strain producing ristocetin. [PDF]
Discovering new antibiotics is a major scientific challenge, made increasingly urgent by the continued development of resistance in bacterial pathogens.
Cheng, Jinhua +5 more
core +3 more sources
Draft Genome Sequence of Amycolatopsis lurida NRRL 2430, Producer of the Glycopeptide Family Antibiotic Ristocetin. [PDF]
We report here the first draft genome sequence for Amycolatopsis lurida NRRL 2430, the producer of the glycopeptide antibiotic ristocetin. The 9-Mbp genome is predicted to harbor 8,143 genes, including those belonging to the ristocetin biosynthesis ...
Hong, Hee-Jeon, Kwun, Min Jung
core +4 more sources
Bleeding because of impaired platelet function is a major side effect of the Bruton’s tyrosine kinase (BTK) inhibitor ibrutinib. We quantitatively assessed ristocetin-induced platelet aggregation (RIPA) in 64 patients with chronic lymphocytic leukemia ...
Alexander Egle
exaly +2 more sources
BACKGROUND Injury to the blood-brain barrier exposes endothelium rich in von Willebrand factor (vWF), which may play a role in altered platelet aggregation following traumatic brain injury (TBI).
Lucy Z Kornblith, Anamaria J Robles
exaly +2 more sources
Thrombocytosis and bleeding in myeloproliferative neoplasms: exploring clinical diversity and risk of acquired von Willebrand syndrome—insights from a UK center [PDF]
Background: Myeloproliferative neoplasms (MPNs) represent a group of blood disorders characterized by myeloid cell proliferation and an associated increased risk of thrombosis and bleeding.
Giulia Simini +8 more
doaj +2 more sources
A rare case of acquired von Willebrand syndrome type 2B: diagnosis, treatment, and underlying pathophysiology [PDF]
Background: Acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder that usually mimics type 1 or 2A von Willebrand disease (VWD). Key Clinical Question: Can AVWS mimic the phenotype of type 2B VWD?
Simon Jaouen +5 more
doaj +2 more sources
Limitations of the ristocetin cofactor assay in measurement of von Willebrand factor function
V. Flood +9 more
exaly +2 more sources

